Evidence map›Paper›PMID 40795996›Full record

ArticleOpen biology2025

Developmental remodelling of

Péter Görög, Tibor Novák, Tamás F Polgár, Péter Bíró, Adél Gutheil, Csaba Kozma, Tamás Gajdos, Krisztina Tóth, Alexandra Tóth, Miklós Erdélyi and 2 more

Abstract read
In one paragraph

Article in Open biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Developmental remodelling ofOpen biology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Péter GörögHUN-REN Biological Research Centre, Szeged, Hungary.
Tibor NovákDepartment of Optics and Quantum Electronics, University of Szeged, Szeged, Hungary.
Tamás F PolgárTransmission Electron Microscope Laboratory, Core Facility, Szeged, Hungary.
Péter BíróDepartment of Optics and Quantum Electronics, University of Szeged, Szeged, Hungary.
Adél GutheilDepartment of Genetics, University of Szeged, Szeged, Hungary.
Csaba KozmaDepartment of Genetics, University of Szeged, Szeged, Hungary.
Tamás GajdosDepartment of Optics and Quantum Electronics, University of Szeged, Szeged, Hungary.ORCID 0000-0002-5288-4659
Krisztina TóthHUN-REN Biological Research Centre, Szeged, Hungary.
Alexandra TóthHUN-REN Biological Research Centre, Szeged, Hungary.
Miklós ErdélyiDepartment of Optics and Quantum Electronics, University of Szeged, Szeged, Hungary.
József MihályHUN-REN Biological Research Centre, Szeged, Hungary.
Szilárd SzikoraHUN-REN Biological Research Centre, Szeged, Hungary.ORCID 0000-0003-4339-4946

Funding

Development, and Innovation OfficeHungarian Academy of SciencesHungarian Science Foundation (OTKA)János BolyaiMinistry of CultureNew National Excellence ProgramNew National Excellence Program of the Ministry for Culture and InnovationThe National Laboratory of BiotechnologyÚNKP
6 · The paper itself

Abstract

The indirect flight muscle is a widely used model for studying sarcomere structure and muscle development due to its extremely regular architecture. Nevertheless, precise measurement of the basic sarcomeric parameters remains a challenge even in this greatly ordered tissue. In this study, we identified several factors affecting measurement reliability and developed a software tool for precise, high-throughput measurement of sarcomere length and myofibril width. The accuracy of this new tool was validated against simulated images and blinded manual measurements. To extend the scope of this morphometric analysis to the sub-sarcomeric scale, we used electron and super-resolution microscopy to quantify myofilament number and filament length during myofibrillogenesis. Our findings revealed the dynamics of thin and thick filament elongation, as well as the addition of myofilaments at the sarcomere periphery during myofibrillogenesis. We precisely measured the dimensions of the Z-disc, I-band and H-zone during development, enabling us to construct refined models of sarcomere growth at the level of individual myofilaments, providing a spatial framework for interpreting nanoscopic localization data. These models deepen our understanding of sarcomere growth and lay the groundwork for future studies on the molecular mechanisms driving myofilament elongation and assembly.

Indexed as

DrosophilaDrosophila melanogasterMuscle DevelopmentMyofibrilsSarcomeresActin CytoskeletonAnimalsFlight, AnimalSoftwareDrosophilaflight musclenanoscopysarcomerethick filamentthin filament

Identifiers

PMID40795996
PMCPMC12343135

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.